Sun Pharmaceutical is hiring Quality Control Officer – B. Pharma/ B. Sc./ M. Sc can apply

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With annual revenues of more than US$ 5.1 billion, Sun Pharmaceutical Industries Ltd. (Sun Pharma) is the fourth-largest specialty generic pharmaceutical firm in the world. With the help of more than 40 production facilities, we supply more than 100 nations with high-quality, reasonably priced medications that are dependable among patients and medical experts.

Position – Officer Quality Control (API)
Grade- G12C
Qualification- M.Sc. / B.Sc./ B.Pharma
Experience- 3 to 5 Year
Candidate from regulatory market will be preferred

Job Description:
1. Analytical Testing: To perform analysis of laboratory samples (Finished API’s, Intermediates, Raw Materials, Recovered Solvent, In-process material, Working Standards) on HPLC/ Wet laboratory instruments as per approved Specification, Test procedures and as per customer requirement.
2. Laboratory Instruments: To perform and ensure all Wet laboratory instruments are maintained and calibrated as per schedule. To perform daily/weekly calibration of wet laboratory instruments as per schedule. To ensure laboratory instruments (HPLC) are maintained and calibrated as per schedule
3. Temperature and Humidity Monitoring QC laboratory and maintain the relevant records.
4. Issuance of analytical raw data sheet for relevant analysis.
5. Inventory: To maintain inventory of laboratory chemical and documents/spares in HPLC laboratory.
6. Sample Handling: Handling and disposal of under test laboratory samples and to ensure that under test laboratory samples are kept as per their recommended conditions and maintain the disposal of under test laboratory samples after completion of analysis.
7. Training: To ensure that continuously upgrade the skills through training and technical inputs for knowledge up gradation to drive continuous improvements in laboratory performance.
8. Safety: To ensure compliance to cGxP and applicable safety standards in the QC laboratory.
9. Verification of general cleaning, destruction of GxP documents and maintenance of related Record. Issuance of analytical raw data sheet and log books for relevant analysis.

Location: Dewas API – Quality Control
Apply Now

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